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Human Disease and Mouse Model Detail
Human Disease Corneal Dystrophy, Gelatinous Drop-Like; GDLD
OMIM ID: 204870
Human Phenotype Ontology associations
Synonyms Amyloid Corneal Dystrophy, Japanese Type; Amyloidosis, Corneal; CDGDL; Corneal Dystrophy; Corneal Dystrophy, Lattice Type III; Lattice Corneal Dystrophy, Type III
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     TACSTD2* Tacstd2   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory